Evidence map›Paper›PMID 40364580›Full record

ArticleCancer science2025

Identification of a Distal Enhancer That Regulates TGF-β-Induced SNAI1 Expression.

Hao Fu, Yuka Itoh, Tomoe Sawaguchi, Shigeo Otake, Chiho Omata, Masao Saitoh, Keiji Miyazawa

Abstract read
In one paragraph

Article in Cancer science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Hao FuDepartment of Biochemistry, Graduate School of Medicine, University of Yamanashi, Chuo, Japan.
Yuka ItohDepartment of Biochemistry, Graduate School of Medicine, University of Yamanashi, Chuo, Japan.
Tomoe SawaguchiDepartment of Biochemistry, Graduate School of Medicine, University of Yamanashi, Chuo, Japan.
Shigeo OtakeDepartment of Biochemistry, Graduate School of Medicine, University of Yamanashi, Chuo, Japan.
Chiho OmataDepartment of Biochemistry, Graduate School of Medicine, University of Yamanashi, Chuo, Japan.
Masao SaitohDepartment of Biochemistry, Graduate School of Medicine, University of Yamanashi, Chuo, Japan.ORCID https://orcid.org/0000-0003-0793-1679
Keiji MiyazawaDepartment of Biochemistry, Graduate School of Medicine, University of Yamanashi, Chuo, Japan.ORCID https://orcid.org/0000-0002-7835-7718

Funding

Japan Science and Technology Agency SPRING JPMJSP2133Japan Society for the Promotion of Science 21H02762Japan Society for the Promotion of Science 23K21385
6 · The paper itself

Abstract

Snail is a zinc finger transcription factor encoded by the SNAI1 gene and triggers a cellular process termed epithelial-mesenchymal transition (EMT) upon its increased expression and/or functional activation. Snail expression and activity are regulated by various extracellular stimuli, including cytokines and environmental factors. Transforming growth factor-β (TGF-β) is a Snail inducer that functions via Smad3-mediated transcriptional activation. In the present study, we identified a distal enhancer that modulates TGF-β-induced SNAI1 expression. ChIP-seq and Hi-C analyses showed that the enhancer is located 46 kb downstream of the SNAI1 gene; in TGF-β-stimulated cells, it associates with Smad3 and interacts with the SNAI1 proximal promoter. Inhibiting the activity of the enhancer using CRISPRi attenuated TGF-β-induced SNAI1 expression, stress fiber formation, and cell motility enhancement, suggesting that the enhancer mediates TGF-β-induced EMT. The enhancer contains a Smad-binding CAGA motif and an activator protein-1 (AP-1) binding motif that function in transcriptional activation. Ras-responsive element binding protein 1 (RREB1), a transcription factor required for TGF-β-induced Snail expression, regulated the basal activity of the enhancer but not its inducibility by TGF-β. In contrast to the enhancer, the association of Smad3 with the proximal promoter was not evident. These findings suggest that the proximal promoter and the distal enhancer respond to distinct signaling cues, integrate them, and cooperatively function to drive SNAI1 expression.

Indexed as

Enhancer Elements, GeneticSnail Family Transcription FactorsTransforming Growth Factor betaCell Line, TumorCell MovementDNA-Binding ProteinsEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansPromoter Regions, GeneticSmad3 ProteinTranscriptional ActivationTranscription FactorsDNA-Binding ProteinsSmad3 ProteinSMAD3 protein, humanSNAI1 protein, humanSnail Family Transcription FactorsTranscription FactorsTransforming Growth Factor betaEMTenhancerSmadsnailTGF‐β

Identifiers

PMID40364580
PMCPMC12317401

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.